U.S. patent number 3,776,239 [Application Number 05/254,195] was granted by the patent office on 1973-12-04 for aspirator needle.
This patent grant is currently assigned to Sherwood Medical Industries Inc.. Invention is credited to Denton A. Cooley.
United States Patent |
3,776,239 |
Cooley |
December 4, 1973 |
ASPIRATOR NEEDLE
Abstract
An aspirator needle for use in open-heart surgery during
cardiopulmonary bypass to reduce the risk of air entrapment in the
aorta. The needle consists of a cannula provided with a pointed end
and an axial slot in the wall thereof extending substantially the
length of the cannula, and a hub configured to connect to a source
of suction via a connecting tube.
Inventors: |
Cooley; Denton A. (Houston,
TX) |
Assignee: |
Sherwood Medical Industries
Inc. (St. Louis, MO)
|
Family
ID: |
22963295 |
Appl.
No.: |
05/254,195 |
Filed: |
May 17, 1972 |
Current U.S.
Class: |
604/117; 604/272;
604/122 |
Current CPC
Class: |
A61B
17/3417 (20130101); A61M 25/0108 (20130101) |
Current International
Class: |
A61B
17/34 (20060101); A61M 25/01 (20060101); A61b
017/34 () |
Field of
Search: |
;128/214R,214B,214.2,221,2F,276-278,347 |
References Cited
[Referenced By]
U.S. Patent Documents
Other References
Groves et al.-Jour. Thorac. & Card. Surg. Vol. 47, No. 3 Mar.
1964 pp. 349-355..
|
Primary Examiner: Truluck; Dalton L.
Claims
What is claimed is:
1. An aspirator needle for insertion into a body vessel comprising
a needle cannula having a pointed distal end, and a hub connected
to a proximal portion of said cannula and having a distal end face,
said cannula having a free portion extending axially from said end
face for a distance less than the diameter of the body vessel to
prevent penetration of the opposed wall of the body vessel when the
aspirator needle is inserted with said end face substantially
engaging the exterior of the body vessel, said free portion having
an axially elongate slot extending through the wall of said cannula
with the proximal end of said slot spaced from said end face to
define therebetween an unslotted portion and to define a slotted
portion between tbe proximal end of said slot and the distal end of
said cannula, said unslotted portion being substantially smaller in
axial length than said slotted portion so that when the aspirator
needle is inserted into the body vessel substantially up to said
end face, the proximal end of said slot is closely adjacent the
interior of the body vessel wall so that air bubbles within the
body vessel adjacent the interior of the body vessel wall can enter
said slot, said hub having a bore therein in fluid communication
with said cannula and means thereon for receiving a flexible tube
in fluid communication with said bore.
2. The aspirator needle set forth in claim 1 wherein said slot
extends continuously from the proximal end of said slot to the
distal end of said cannula.
3. The aspirator needle set forth in claim 1 wherein said unslotted
portion is cylindrical and has an axial length approximately equal
to the average thickness of the body vessel wall.
4. The aspirator needle set forth in claim 3 wherein said slot
extends continuously from the proximal end of said slot to the
distal end of said cannula.
5. The aspirator needle set forth in claim 1 wherein the axial
length of said unslotted portion is approximately .078 inch and the
axial length of said slotted portion is approximately .422
inch.
6. The aspirator needle set forth in claim 5 wherein said slot
extends continuously from the proximal end of said slot to the
distal end of said cannula.
7. The aspirator needle set forth in claim 1 wherein the axial
length of said hub is at least two times the length of said free
portion of said cannula.
Description
BACKGROUND OF THE INVENTION
This invention relates to medical devices, and more particularly to
a disposable aspirator needle for use in eliminating air embolism
during cardiopulmonary bypass procedures.
In an article entitled "A Needle-Vent Safeguard Against Systemic
Air Embolus in Open-Heart Surgery," written by Doctors L.K. Groves
and D.B. Effler for the Department of Thoracic Cardiovascular
Surgery, The Cleveland Clinic Foundation, Cleveland, Ohio, the
dangers of entrapment of air in the left side of the heart, which
may then enter the systemic circulation, is discussed in great
detail. Briefly, as this article points out, in most open-heart
procedures the highest point in the central cardiovascular system
is the ascending aortic arch between the aortic valve ring and the
innominate artery takeoff, and that any air accumulating in the
circulatory system during an operative procedure will of necessity
flow along the upper surface of the aorta and form a bubble at this
highest point. An air bubble that reaches this aortic arch may
enter the innominate artery and thus gain access to the right
carotid artery circulation and cause neurologic deficits in the
left half of the body.
While air or other gases may also accumulate in other portions of
the cardiovascular system adjacent the heart during cardiopulmonary
bypass, and while considerable quantities of air can frequently be
tolerated in the systemic circulation without causing obvious
complications, it is well known that a minute embolus carried to a
strategic location may cause tragic consequences.
While the above article describes a vent needle suitable for use in
removing air entrapped in the aortic arch, and while many issued
patents, such as U.S. Pat. No. 3,076,457, disclose aspirating
needles which may possibly be used for this purpose, none of these
prior art devices have proven entirely satisfactory for the
purposes hereinbefore described.
SUMMARY OF THE INVENTION
Accordingly, it is an object of the present invention to provide an
aspirator needle which permits rapid and effective aspiration of
air trapped in the cardiovascular system during cardiopulmonary
bypass procedures.
It is another object of this invention to provide such an
aspirating needle which substantially eliminates the disadvantages
of prior art devices, and which is characterized by simplicity of
construction, and ease of operation and use.
A still further object of this invention is to provide such a
needle which is of economical construction for disposal after but a
single use, but which is highly effective and safe.
An aspirator needle constructed in accordance with the present
invention is comprised of a needle cannula having a point at its
distal end and an elongate slot extending axially through tbe wall
of the cannula over substantially the entire length thereof. A hub,
having an axial bore therein, is provided with a distal end portion
receiving the butt end of the needle cannula in fluid flow
communication with the bore of the hub. The hub further comprises
an elongate generally cylindrical center portion and a proximal end
portion, the latter having means thereon for detachably receiving a
flexible tube over the periphery of the proximal end portion of the
hub.
These and other objects and features will be in part apparent and
in part pointed out hereinafter.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a longitudinal view of the aspirator needle of this
invention;
FIG. 2 is an enlarged transverse sectional view taken on lines 2--2
of FIG. 1; and
FIG. 3 is a diagramatic view of the aspirator needle of this
invention as it is used.
Corresponding reference characters indicate corresponding parts
throughout the several views of the drawings.
DESCRIPTION OF THE PREFERRED EMBODIMENT
Referring now to the drawings, and particularly to FIG. 1, the
present aspirator needle, generally indicated at 10, is shown to
comprise a needle cannula 12 and a hub 14. The needle cannula 12 is
of elongate, cylindrical configuration having a bevel point 16 at
its distal end and an elongate slot 18 extending axially through
the wall of the cannula over substantially the entire length
thereof. As illustrated in FIG. 1 of the drawings, the slot 18
terminates at the butt end 20 of the needle just short of the hub
14, and is embedded in the hub and attached thereto by any suitable
means, such as by an epoxy adhesive.
The hub 14 is comprised of a cylindrical distal end portion 22, an
elongate center portion 24 and a proximal end portion 25. As
illustrated in the drawings, center section 24 is provided with
four axially extending ribs 27 to assist in grasping the needle,
and proximal end portion 25 is provided with three peripherally
extending circular tube retaining ridges 26, each of which tapers
from a maximum diameter at its distal end to a minimum diameter at
its proximal end substantially coextensive with the surface of the
proximal end portion 25 of the hub. While three such tube retaining
ridges have been illustrated and described, it should be understood
that any suitable number may be provided for securing the tube to
the proximal end portion of the needle hub 14. The hub 14 is
further provided with substantially planar proximal and distal end
faces 28 and 30, respectively. In addition, a peripherally
extending enlarged diameter shoulder 32 is provided on the needle
hub intermediate the center and proximal end portions thereof which
serves as a tube stop, as will be described more fully hereinafter.
As illustrated by dotted lines 34 in FIG. 1, the hub has a tapering
axial bore extending throughout its length in fluid flow
communication with the butt end 20 of needle cannula 12. The
proximal end of the bore 34 is open at face 28 of the hub.
The needle cannula 12 and hub 14 are preferably formed of stainless
steel and a suitable synthetic resinous material such as
polypropylene, respectively, to provide an assembly of low cost so
that the aspirator needle may be disposed of after a single use. As
illustrated in FIG. 1, the aspirator needle is preferably 21/2
inches in overall length with the hub portion 14 extending
approximately 2 inches and the free length of the needle cannula
extending from the distal face 30 of the hub approximately 1/2
inch. This provides an assembly which is easily manipulated for
insertion and retraction of the needle cannula through the wall of
the aorta, or other body vessel, without extending completely
through both walls of the vessel. In addition, the free length of
the butt end 20 of the needle cannula 12 is approximately 0.078
inches in axial dimension to ensure that this portion of the needle
cannula extends completely through the wall of the aorta to prevent
aspiration of the vessel tissues into the slot 18.
As illustrated in FIG. 3 of the drawings, the aspirator needle 10
is detachably connected to a flexible aspirating tube 36 by
telescoping the end of the tubing over the proximal end portion 25
of the needle hub into abutment with shoulder 32. The tube
retaining ridges 26 securely retain the tube on the proximal end
portion of the hub to prevent inadvertent disassembly thereof. With
the tube 36 connected to the needle hub portion 25, and with the
tubing 36 connected to a suitable aspirating pump or source of
negative pressure, the needle cannula 12 is inserted through the
wall 38 of the aorta for aspiration of air bubbles, such as those
indicated at 40, trapped therein. Since the slot 18 extends over
substantially the entire length of the needle cannula 12, all of
the air trapped in the aortic arch, including that along the
uppermost surface of the aortic wall, will be removed. Furthermore,
the slotted needle facilitates removal of air bubbles with a small
puncture. In addition, since the butt end 20 of the needle cannula
12 is unslotted, the aortic wall 38 will not be damaged by
aspiration into the needle.
Th present needle may be used at the conclusion of cardiopulmonary
bypass to reduce the risk of air entrapment in the aorta when going
off bypass or continuously throughout the operative procedure,
depending on the particular procedure performed by the surgeon.
While some blood loss will occur through the needle, depending upon
the perfusion pressure used, this blood may be returned to the
patient through either the cardiotomy reservoir or the
oxygenator.
In view of the above, it will be seen that the several objects of
the invention are achieved and other advantageous results
obtained.
As various changes could be made in the above constructions without
departing from the scope of the invention, it is intended that all
matter contained in the above description or shown in the
accompanying drawings shall be interpretted as illustrative and not
in a limiting sense.
* * * * *